D58.9 Hereditary hemolytic anemia, unspecified
Billable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.
Applies from D58 Other hereditary hemolytic anemias
Excludes1 (never code together)
- hemolytic anemia of the newborn (P55.-)
Risk adjustment (HCC)
- CMS-HCC V22: HCC 48 — Coagulation Defects and Other Specified Hematological Disorders
- ESRD V24: HCC 48
MS-DRG index
Defines the logic of DRG(s) 811-812 in MDC 16.
Approximate ICD-9-CM (GEMs)
282.9 Hereditary hemolytic anemia, unspecified
Code annotations containing back-references to D58.9
Back-references to D58
- Type 1 Excludes:
D57 Sickle-cell disorders ("other hemoglobinopathies (D58.-)") - Code First:
M90.5 Osteonecrosis in diseases classified elsewhere ("hemoglobinopathy (D50-D64)") - Type 1 Excludes:
R71 Abnormality of red blood cells ("anemias (D50-D64)")
Diagnosis Index entries for D58.9
- Abnormal, abnormality, abnormalities › erythrocytes › congenital, with perinatal jaundice
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › childhood
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › chronic › hemolytic
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › congenital › hereditary hemolytic NOS
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › hemolytic
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › hemolytic › chronic
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › hemolytic › familial
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) › hemolytic › hereditary
Nearby codes
D58 Other hereditary hemolytic anemiasD58.0 Hereditary spherocytosisD58.1 Hereditary elliptocytosisD58.2 Other hemoglobinopathiesD58.8 Other specified hereditary hemolytic anemiasD58.9 Hereditary hemolytic anemia, unspecified (this code)